Tag | Content |
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EnhancerAtlas ID | HS091-47980 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr9:97084610-97086850 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr9:97086551-97086563 | AAACAAACAAAC | - | 6.32 | IRF1 | MA0050.2 | chr9:97086648-97086669 | TTATTGAAAGTGAAAGCCAGG | - | 6.3 | RUNX1 | MA0002.2 | chr9:97085730-97085741 | AAACCACAAAC | - | 6.02 | Zfx | MA0146.2 | chr9:97086704-97086718 | GAGGCCGAGGCGGG | - | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | GCTGTAAACC AGTGCAGTCA GTCCCAGTCT GTAAGCCCAC CCTCCATCCC GGGCCCACCT 60 GGTCCCAACA CCTGGCTCCT GTCCTCCCCA CACCTGTCCT GCCATCTGTC CCTGTCCTGT 120 TCTCCCCCAT GTGGGCTCCT CAGCCTCCAG GACACACCCC CAAGATCCAA CATCAATAGA 180 AGCCACTGAG TGGCCTCTCC GACTGCCTCT CAAGTCCTCG GTGTTATGAT GTTGACAAGC 240 GAACTCAGTG CTATGGGTGG AACATGTGTG TCCCCAACAT TCCTGTGCTG AAGCCCTCAG 300 TGTCAGTGTG TCAGTATTTG GAGGCAATCA GGGTTAGAGC AGGTCATGAG CGTGGGTCCC 360 AGTCATGGAA TCCGAGCTCT GATAAGGGCA GGAGGAGACA CCAGGGCTCT TGCTCTCAGC 420 CACAAGAGCA CACAGCCAGA GGCAGCTCTC TCCAGCCAGG AAGAGGGCCC TGACCAGACA 480 CCCAATCCGC TGTCACCTTG ATCTGGGACT TCTGGCCTCT GGAACTAGGA GACATGAATG 540 TGTCTTGATA AAGCACCCAG TCTATGGGAT TCGTTACGGC AGAGCCTGAG CTGACTGAGA 600 CACCATGCAC ACAGAATGAC CTGGGAGCGA GGGTTAAAGT GCAGGTTCCT GGGCCACAGG 660 ACTGAGCATT TAACCAGCTT CCTGGGGACT CTGGAGCAAG GCAGCCCCTG GGGACACAGC 720 CTCAGGGTCC TGGAGCTTGA GGAGCAGGAG CACACGTCCA GAACCAAAGC AGAGCGGTGT 780 CCAAGCCACT GCAAGCAGCC AGGCACAGCT TCCCACATTC CCACAGGAGC CAAGGCAAAG 840 GCCTGTGAGC CCGGGGCGGC TACACTCCAA GAATCAGGGT CCCCAGTGCA CCGGGACTCC 900 GCTCCAAGGG GGGATGCAAC CAGTTCCAGG GTGTGGGGGC AGCGAGACTG TTGGGGAGGA 960 AGACGGGGCC GCCTTCACCT ACACCCCAGG CAGGGGACTC CCCTAGGGGA ATGGCCAGTG 1020 TGTTGCACGG TGGATATGCT CAAGCTCCTG TTTGCTCATC AGCGGGAAAC ACAGGGTCAC 1080 AGAGGTGCCG CGGGGTGGAG AGAGGCAGGG ACTGGGAATG AAACCACAAA CTCTCCCAGA 1140 TGCTGATGTT GCTGCCTCAC AGTCACCACA GTCCACGGCT CTGGGCTGCT GGGCTCGTGG 1200 TGCACTCAGA GCTATCACTG GAGCCCGTGG CTTTGGGGAG CACTCTCCTA GATGGCCTAG 1260 TCCTGATAAT GGTAGTAATG GGGACAGTAA TCATAACTGC TGTCATGTAA TGTGTCATAG 1320 TATGTGCCAG GCACTGTGCT ACGTATGTCA TATGTGAGCT CAGGTCATCT CTTTGCCATC 1380 CTCTGAATGA AACACCATTG TCCTTTTTTC TAGGGGGGAT TGACGGTGAA GATGCTAATA 1440 CCTGCCCAGC ATCGACCCTA GTGCGGGTCC CAAGACCATC CCCCTGTGCA GGCTCCACCA 1500 CCGCTGTGCT AACTGGACCG CGGCAGAACA GTGTGGGTGT GTGCCAGGTT CCTGCTGGGC 1560 CCTGCAGCTC CTCCCCCCAG CCCCATGTGA TGTGCCCCTG GCCATTGACA CTCAGTTCGA 1620 GGGAAGGCAC TGGGGTGTAC ACTCAAAGAC CTAAACCCAG GGTGGGTGCG GTGGCTCACG 1680 CCTGCAATCC TAGCACTTTG GGAGGCTGAG GCGGGTGGAT CACAAAGTCA GGAGTTCAAG 1740 ACCAGCCTGC TCAACATAGT GAAACCCCGT CTCTACTAAA AAATACAAAA AATTAGCTGG 1800 GCATGGTGGC GGGCGCCTGT AAGCCCAGGT ACTTGGGAGG CTGAGGCAGG AGAATCGCTT 1860 GAACCTAGGA GGCAGAGGTT GCGGTGAGCC AAGATCTCAC CATTGCACTC CAGCCTGGGT 1920 GACAGTGCGA GACTCCATCT CAAACAAACA AACAAAAAAG ACCTAAACCC TAACCGTGGC 1980 TCATGTCACA CCAAGAACGC TCTCTGACCT GGGTCTTCTG TAAACATTGT TGTGAAAATT 2040 ATTGAAAGTG AAAGCCAGGC ACGGTGGCTC ATGCCTGCAA TCGCAGCACT TTGGGAGGCC 2100 GAGGCGGGCG AATCACCAGG GCAGGAGATT GAGAGCATCC TGGCTAACAT GGTGAAACCC 2160 CGTCTCTACT AAAAATACAA AAAAATTAGC CGGGCATGGT GGTGGGCACC TGTAGTCCCA 2220 GCTACTCGGG AGCCTGAGGC 2240
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